Canonical Allele Identifier: CA1949567467
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226593T= , CM000673.2:g.5226593T= GRCh38
NC_000011.9:g.5247823T= , CM000673.1:g.5247823T= GRCh37
NC_000011.8:g.5204399T= NCBI36
NG_000007.3:g.71023A=
NG_059281.1:g.5479A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.299A= ENSP00000494175.1:p.Asp100=
ENST00000335295.4:c.299A= MANE Select ENSP00000333994.3:p.Asp100=
ENST00000475226.1:n.231A=
ENST00000485743.1:n.350A=
ENST00000633227.1:c.*115A= ENSP00000488004.1:n.*115A=
NM_000518.4:c.299A= NP_000509.1:p.Asp100=
NM_000518.5:c.299A= MANE Select NP_000509.1:p.Asp100=